Carbohydrate antigen 125 concentrations across the ejection fraction spectrum in chronic heart failure: The EMPEROR programme

Author:

Ferreira João Pedro123,Packer Milton45,Sattar Naveed6,Butler Javed78,Pocock Stuart J.9,Anker Stefan D.10,Maldonado Sandra González11,Panova‐Noeva Marina12,Sumin Mikhail13,Masson Serge14,Zannad Faiez15,Januzzi James L.16ORCID

Affiliation:

1. Department of Surgery and Physiology Faculty of Medicine of the University of Porto, Cardiovascular Research and Development Center (UnIC@RISE) Porto Portugal

2. Heart Failure Clinic, Internal Medicine Department, Centro Hospitalar de Vila Nova de Gaia/Espinho Gaia Portugal

3. Centre d'Investigations Cliniques Plurithématique 14‐33, Inserm U1116, CHRU, F‐CRIN INI‐CRCT (Cardiovascular and Renal Clinical Trialists), Cardiovascular Research and Development Center Université de Lorraine Nancy France

4. Imperial College London London UK

5. Baylor Heart and Vascular Institute, Baylor University Medical Center Dallas TX USA

6. School of Cardiovascular and Metabolic Health, University of Glasgow Glasgow UK

7. Baylor Scott and White Research Institute Dallas TX USA

8. University of Mississippi Medical Center Jackson MS USA

9. London School of Hygiene and Tropical Medicine London UK

10. Center for Regenerative Therapies Berlin Institute of Health, Department of Cardiology, German Centre for Cardiovascular Research, partner site Berlin, Charité Universitätsmedizin Berlin Berlin Germany

11. Boehringer Ingelheim Pharma GmbH & Co. KG Biberach Germany

12. Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Germany

13. Boehringer Ingelheim International GmbH Ingelheim Germany

14. Roche Diagnostics International Ltd Rotkreuz Switzerland

15. Centre d'Investigations Cliniques Plurithématique 1433, INSERM Université de Lorraine Nancy France

16. Massachusetts General Hospital and Baim Institute for Clinical Research Boston MA USA

Abstract

AimVascular congestion may lead to an increase of carbohydrate antigen 125 (CA‐125). The role of CA‐125 as a biomarker of congestion or for prognosis across the full ejection fraction (EF) spectrum of chronic heart failure (HF) remains unknown.Methods and resultsSerum CA‐125 was measured in 1111 study participants from the EMPEROR‐Reduced and EMPEROR‐Preserved trials. Congestive signs and symptoms were evaluated across CA‐125 tertiles. Cox regression was used to study the association with outcomes. The primary outcome was a composite of first HF hospitalization or cardiovascular (CV) death. No significant association was present between baseline CA‐125 levels and congestive signs or symptoms. In the overall population, higher CA‐125 levels were not associated with an increased risk of primary outcome (tertile 3 vs. tertile 1: hazard ratio [HR] 1.34; 95% confidence interval [CI] 0.91–1.96; p‐trend = 0.11). However, higher CA‐125 levels were associated with an increased risk of primary outcome in patients with HF and reduced EF (HFrEF; tertile 3 vs. tertile 1: HR 2.25 [95% CI 1.30–3.89]), but not among patients with preserved EF (HFpEF; tertile 3 vs. tertile 1: HR 0.68 [95% CI 0.38–1.21]); interaction‐p = 0.02). Patients in the upper CA‐125 tertile also showed the steepest estimated glomerular filtration rate decline over time (p‐trend = 0.03). The effect of empagliflozin to reduce the risk of CV death or HF hospitalization appeared to be attenuated in those with lower baseline CA‐125 levels (interaction‐p‐trend = 0.09).ConclusionAcross the range of EF in patients with chronic HF enrolled in the EMPEROR trials, the majority of whom did not have clinical evidence of congestion, CA‐125 concentrations were not significantly associated with congestive signs or symptoms. CA‐125 concentrations may predict HF hospitalization/CV death in patients with HFrEF, but not those with HFpEF.Clinical Trial Registration: EMPEROR‐Reduced (NCT03057977), EMPEROR‐Preserved (NCT03057951).

Publisher

Wiley

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